(+)-Epichlorohydrin → tert-Butyl (2S)-2-[(4-cyanophenoxy)methyl]-1-aziridinecarboxylate
Reaktionsgleichung
[C:1]([C:3]1[CH:20]=[CH:19][C:6]([O:7][CH2:8][CH:9]2[CH2:11][N:10]2[C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])=[CH:5][CH:4]=1)#[N:2].C([C@H]1OC1)Cl>>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([O:7][CH2:8][C@@H:9]2[CH2:11][N:10]2[C:12]([O:14][C:15]([CH3:16])([CH3:17])[CH3:18])=[O:13])=[CH:19][CH:20]=1)#[N:2]Komponenten
3
Versuchsvorschrift
The sub-title compound was prepared according to the procedures described in steps (i) to (v) above for the synthesis of tert-butyl 2-[(4-cyanophenoxy)methyl]-1-aziridinecarboxylate, but using (S)-(+)-epichlorohydrin in place of epichlorohydrin in step (i).
Quellen und Nachweise
- ORD-Eintrag
- ord-b9e5235c2d3240e8853c057e06b9423c
- Quelldatensatz
- uspto-grants-2008_04
- Patentnummer
- US07351821B2
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